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Polyoxalate Nanoparticles as a Biodegradable and Biocompatible Drug Delivery Vehicle

机译:聚草酸酯纳米颗粒作为可生物降解和生物相容的药物传递载体

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摘要

One of major challenges in the drug delivery lies in the development of nanoparticles that are effectively delivered to targeted cells and release their payload over an extended period to achieve a clinical response. In this paper, we report a new family of biocompatible and biodegradable polymer, termed polyoxalate that degrades hydrolytically into nontoxic byproducts. Polyoxalate was synthesized from a simple one-step polymerization reaction of 1,4-cyclohexanedimethanol and oxalyl chloride and had a MW of ~11000 Da. This polymer was designed to degrade by water hydrolysis into 1,4-cyclohexanedimethanol and oxalic acid, which can be easily removed from a body. Polyoxalate had a hydrophobic backbone and was formulated into nanoparticles with a mean diameter of 600 nm, which is suitable for drug delivery involving phagocytosis by macrophages. Polyoxalate nanoparticles were readily taken up by RAW 264.7 macrophage cells and HEK (human embryonic kidney) 293 cells and exhibited a minimal cytotoxicity in a time- and dose-dependent manner. In comparison with PLGA nanoparticles, polyoxalate nanoparticles had a significantly higher cell viability. We anticipated that the ease of synthesis and excellent biocompatibility make polyoxalate highly potent for numerous applications in drug delivery.
机译:药物递送中的主要挑战之一是开发可有效递送至靶细胞并在延长的时间内释放其有效载荷以实现临床反应的纳米颗粒。在本文中,我们报告了一个新的生物相容性和可生物降解聚合物家族,称为聚草酸酯,它可以水解降解为无毒副产物。聚草酸酯是通过简单的一步聚合1,4-环己烷二甲醇与草酰氯的反应合成的,分子量为〜11000 Da。该聚合物经设计可通过水解降解为1,4-环己烷二甲醇和草酸,可轻松从体内去除。聚草酸酯具有疏水性骨架,并被配制成平均直径为600 nm的纳米颗粒,适用于涉及巨噬细胞吞噬作用的药物输送。聚草酸酯纳米颗粒易于被RAW 264.7巨噬细胞和HEK(人类胚胎肾脏)293细胞吸收,并以时间和剂量依赖性方式表现出最小的细胞毒性。与PLGA纳米颗粒相比,聚草酸酯纳米颗粒具有明显更高的细胞活力。我们预期合成的简便性和出色的生物相容性使聚草酸酯在药物递送的众多应用中具有很高的效力。

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